ID   SW480 EGFP-lamin A clone 11
AC   CVCL_E5G2
SY   SW480 GFP-lamin A clone 11
DR   CancerTools; 162195
RX   PubMed=18714339;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:583; APC; Simple; p.Gln1338Ter (c.4012C>T); ClinVar=VCV000000801; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Val (c.35G>T); ClinVar=VCV000012583; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg273His (c.818G>A); ClinVar=VCV000012366; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Pro309Ser (c.925C>T); ClinVar=VCV000458575; Zygosity=Heterozygous (from parent cell line).
CC   Genetic integration: Method=Transfection; Gene=FPbase; R9NL8; eGFP (Note=Enhanced GFP).
CC   Genetic integration: Method=Transfection; Gene=HGNC; HGNC:6636; LMNA.
CC   Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo.
CC   Derived from site: In situ; Colon; UBERON=UBERON_0001155.
DI   NCIt; C4349; Colon adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0546 ! SW480
SX   Male
AG   51Y
CA   Cancer cell line
DT   Created: 10-04-25; Last updated: 10-04-25; Version: 1
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RX   PubMed=18714339; DOI=10.1371/journal.pone.0002988; PMCID=PMC2496895;
RA   Willis N.D., Cox T.R., Rahman-Casans S.F., Smits K.M., Przyborski S.A.,
RA   van den Brandt P.A., van Engeland M., Weijenberg M.P., Wilson R.G.,
RA   de Bruine A.P., Hutchison C.J.;
RT   "Lamin A/C is a risk biomarker in colorectal cancer.";
RL   PLoS ONE 3:e2988.1-e2988.9(2008).
//